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Terminated Phase 3 Interventional Results available

A Trial to Determine the Efficacy and Safety of Presendin in IIH

ClinicalTrials.gov ID: NCT05347147

Public ClinicalTrials.gov record NCT05347147. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:46 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Randomised, Placebo-controlled, Double-blind, Multi-centre, Clinical Trial to Determine the Efficacy and Safety of Presendin in Idiopathic Intracranial Hypertension

Study identification

NCT ID
NCT05347147
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Invex Therapeutics Ltd.
Industry
Enrollment
14 participants

Conditions and interventions

Interventions

  • Presendin Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 17, 2022
Primary completion
Sep 17, 2023
Completion
Oct 19, 2023
Last update posted
Apr 23, 2024

2022 – 2023

United States locations

U.S. sites
7
U.S. states
6
U.S. cities
7
Facility City State ZIP Site status
UCHealth Sue Anschutz-Rodgers Eye Center - Anschutz Medical Campus Aurora Colorado 80045
University of Miami Leonard M. Miller School of Medicine (UMMSM) - Bascom Palmer Eye Institute Miami Florida 33136
University of Minnesota Health Minneapolis Minnesota 55455
New York Eye and Ear Infirmary of Mount Sinai New York New York 10075
Vanderbilt Eye Institute Nashville Tennessee 37232
The University of Texas Southwestern Medical Center Dallas Texas 75390
Neuro-Eye Clinical Trials, Inc Houston Texas 77074

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05347147, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 23, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05347147 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →